Benign recurrent intrahepatic cholestasis

disorder

SNOMED 31155007CUI C0149841

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal liver enzymes

Very frequent (80-99%)HP:0002910

Cholestatic liver disease

Very frequent (80-99%)HP:0002611

Discolored, acholic stools

Very frequent (80-99%)HP:0011985

Obsessive dieting

Very frequent (80-99%)HP:0002039

Skin itching

Very frequent (80-99%)HP:0000989

Tiredness

Very frequent (80-99%)HP:0012378

Weight loss

Very frequent (80-99%)HP:0001824

Yellowing of the skin

Very frequent (80-99%)HP:0000952

Nausea and vomiting

Frequent (30-79%)HP:0002017

Chronic diarrhoea

Occasional (5-29%)HP:0002028

Cirrhosis

Occasional (5-29%)HP:0001394

Deafness

Occasional (5-29%)HP:0000365

Gallstones

Occasional (5-29%)HP:0001081

Increased hepatocellular carcinoma risk

Occasional (5-29%)HP:0001402

Pancreatitis

Occasional (5-29%)HP:0001733

Upset stomach

Occasional (5-29%)HP:0002027

Related Conditions

Benign intrahepatic cholestasis type 1(child)

Benign intrahepatic cholestasis type 2(child)

Digestive system hereditary disorder(parent)

Hepatopathy(parent)

Disease of biliary system(parent)

Recurrent disease(parent)

Autosomal hereditary disorder(parent)

Quick Facts

SNOMED CT: 31155007
UMLS CUI: C0149841
Fully Specified Name: Benign recurrent intrahepatic cholestasis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.